JUDITH H. VEIS, M.D.; ROBERT CONTIGUGLIA, M.D.; MELVYN KLEIN, M.D.; JEFFREY MISHELL, M.D.; ALLEN C. ALFREY, M.D.; JOSEPH I. SHAPIRO, M.D.
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To the editor: Deferoxamine has been increasingly used to treat iron and aluminum overload in uremic patients on dialysis. Because of the lack of renal function, the half-life of deferoxamine and its chelates, feroxamine and aluminoxamine, is markedly prolonged in this population (1). Although this action improves the effectiveness of chelation, toxicity could also be increased.
We recently saw fatal fungal infections in two nondiabetic patients among our patients on chronic dialysis who were receiving deferoxamine therapy. These patients had received deferoxamine for aluminum-associated bone disease for 4 months and 1 year, respectively. They were receiving a dose of 2
VEIS JH, CONTIGUGLIA R, KLEIN M, et al. Mucormycosis in Deferoxamine-Treated Patients on Dialysis. Ann Intern Med. 1987;107:258. doi: 10.7326/0003-4819-107-2-258_1
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Published: Ann Intern Med. 1987;107(2):258.
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